Drug recall
Apheresis PF24 Plasma
FDA recall event 82771 · Class III · Mississippi Valley Regional Blood Center
Key facts
| Event ID | 82771 |
|---|---|
| Recall numbers | B-0581-2019 |
| Recalling firm | Mississippi Valley Regional Blood Center |
| Product type | Biologics |
| Products | Apheresis PF24 Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Misbranded plasmapheresis product was distributed. |
| Initiation date | Mar 13, 2019 |
| Report date | May 29, 2019 |
| Termination date | May 23, 2019 |
| City | Urbana |
| State | IL |
| Country | United States |
| FEI number | 1470270 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: